Cleared Traditional

K873275 - EXTENSION TABLE 1417
(FDA 510(k) Clearance)

Sep 1987
Decision
31d
Days
Class 1
Risk

K873275 is an FDA 510(k) clearance for the EXTENSION TABLE 1417. This device is classified as a Table, Surgical With Orthopedic Accessories, Manual (Class I - General Controls, product code JEB).

Submitted by Stierlen-Maquet AG (West Germany, GR). The FDA issued a Cleared decision on September 17, 1987, 31 days after receiving the submission on August 17, 1987.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4950.

Submission Details

510(k) Number K873275 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 1987
Decision Date September 17, 1987
Days to Decision 31 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary

Device Classification

Product Code JEB — Table, Surgical With Orthopedic Accessories, Manual
Device Class Class I - General Controls
CFR Regulation 21 CFR 878.4950

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